A new tridentate sulfur receptor as a highly sensitive and selective fluorescent sensor for Cu2+ ions

Chemistry - An Asian Journal

Volumn 8, Issue 11, 2013, Pages 2762-2767

  She, Haiying ^a   Song, Fengling ^a   Xu, Juan ^a   Xiong, Xiaoqing ^a   Chen, Gengwen ^a   Fan, Jiangli ^a   Sun, Shiguo ^a   Peng, Xiaojun ^a  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

copper; fluorescence; reduction; sensors; spiro compounds

Indexed keywords

DETECTION MECHANISM; FLUORESCENT SENSORS; HIGH SENSITIVITY; RAPID RESPONSE TIME; REDUCTION REACTION; SENSING MECHANISM; SPIRO COMPOUNDS; TRIDENTATE RECEPTORS;

CHEMICAL SENSORS; COPPER; FLUORESCENCE; IRON COMPOUNDS; LIGANDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POSITIVE IONS; REDUCTION; SENSORS; SULFUR;

COPPER COMPOUNDS;

COORDINATION COMPOUND; COPPER; FLUORESCEIN DERIVATIVE; FLUORESCENT DYE; ION; PHOSPHOROTHIOIC ACID DERIVATIVE; RHODAMINE; SPIRO COMPOUND; SULFUR;

ARTICLE; CHEMISTRY; CONFORMATION; FLUORESCENCE; OXIDATION REDUCTION REACTION; REDUCTION; SENSORS; SPECTROFLUOROMETRY; SYNTHESIS;

COPPER; FLUORESCENCE; REDUCTION; SENSORS; SPIRO COMPOUNDS;

COORDINATION COMPLEXES; COPPER; FLUORESCEINS; FLUORESCENT DYES; IONS; MOLECULAR CONFORMATION; ORGANOTHIOPHOSPHORUS COMPOUNDS; OXIDATION-REDUCTION; RHODAMINES; SPECTROMETRY, FLUORESCENCE; SULFUR;

EID: 84887019982     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201300534     Document Type: Article

References (50)

1. M. Linder, M. Hazegh-Azam, Am. J. Clin. Nutr. 1996, 63, 797S-811S.
2. C. Vulpe, B. Levinson, S. Whitney, S. Packman, J. Gitschier, Nat. Genet. 1993, 3, 7-13
3. P. C. Bull, G. R. Thomas, J. M. Rommens, J. R. Forbes, D. W. Cox, Nat. Genet. 1993, 5, 327-337.
4. J. S. Valentine, P. J. Hart, Proc. Natl. Acad. Sci. USA 2003, 100, 3617-3622.
5. K. J. Barnham, C. L. Masters, A. I. Bush, Nat. Rev. Drug Discovery 2004, 3, 205-214
6. D. R. Brown, H. Kozlowski, Dalton Trans. 2004, 1907-1917.
7. V. Dujols, F. Ford, A. W. Czarnik, J. Am. Chem. Soc. 1997, 119, 7386-7387
8. R. Krämer, Angew. Chem. 1998, 110, 804-806
9. Angew. Chem. Int. Ed. 1998, 37, 772-773.
10. Y. Zheng, X. Cao, J. Orbulescu, V. Konka, F. M. Andreopoulos, S. M. Pham, R. M. Leblanc, Anal. Chem. 2003, 75, 1706-1712
11. Y. Li, C. M. Yang, Chem. Commun. 2003, 2884-2885
12. Y. Zheng, K. M. Gattas-Asfura, V. Konka, R. M. Leblanc, Chem. Commun. 2002, 2350-2351
13. L. Fabbrizzi, M. Licchelli, P. Pallavicini, A. Perotti, A. Taglietti, D. Sacchi, Chem. Eur. J. 1996, 2, 75-82
14. J. Xie, M. Ménand, S. Maisonneuve, R. Métivier, J. Org. Chem. 2007, 72, 5980-5985
15. A. Torrado, G. K. Walkup, B. Imperiali, J. Am. Chem. Soc. 1998, 120, 609-610
16. Y. Zheng, Q. Huo, P. Kele, F. M. Andreopoulos, S. M. Pham, R. M. Leblanc, Org. Lett. 2001, 3, 3277-3280
17. H. Mu, R. Gong, Q. Ma, Y. Sun, E. Fu, Tetrahedron Lett. 2007, 48, 5525-5529.
18. G.-K. Li, Z.-X. Xu, C.-F. Chen, Z.-T. Huang, Chem. Commun. 2008, 1774-1776
19. K. M. K. Swamy, S.-K. Ko, S. K. Kwon, H. N. Lee, C. Mao, J.-M. Kim, K.-H. Lee, J. Kim, I. Shin, J. Yoon, Chem. Commun. 2008, 5915-5917
20. Z.-C. Wen, R. Yang, H. He, Y.-B. Jiang, Chem. Commun. 2006, 106-108
21. J. Liu, Y. Lu, J. Am. Chem. Soc. 2007, 129, 9838-9839
22. M. Royzen, Z. Dai, J. W. Canary, J. Am. Chem. Soc. 2005, 127, 1612-1613
23. R. Martínez, F. Zapata, A. Caballero, A. Espinosa, A. Tárraga, P. Molina, Org. Lett. 2006, 8, 3235-3238
24. Y. Xiang, A. Tong, P. Jin, Y. Ju, Org. Lett. 2006, 8, 2863-2866
25. Z. Xu, X. Qian, J. Cui, Org. Lett. 2005, 7, 3029-3032
26. X. Zhang, Y. Shiraishi, T. Hirai, Org. Lett. 2007, 9, 5039-5042
27. Y. Zhou, F. Wang, Y. Kim, S.-J. Kim, J. Yoon, Org. Lett. 2009, 11, 4442-4445
28. X. Chen, M. J. Jou, H. Lee, S. Kou, J. Lim, S.-W. Nam, S. Park, K.-M. Kim, J. Yoon, Sens. Actuators B 2009, 137, 597-602
29. L. Mei, Y. Xiang, N. Li, A. Tong, Talanta 2007, 72, 1717-1722
30. E. J. Jun, H. N. Won, J. S. Kim, K.-H. Lee, J. Yoon, Tetrahedron Lett. 2006, 47, 4577-4580.
31. Y. Li, X. Zhang, B. Zhu, J. Xue, Z. Zhu, W. Tan, Analyst 2011, 136, 1124-1128
32. H. S. Jung, P. S. Kwon, J. W. Lee, J. I. Kim, C. S. Hong, J. W. Kim, S. Yan, J. Y. Lee, J. H. Lee, T. Joo, J. S. Kim, J. Am. Chem. Soc. 2009, 131, 2008-2012
33. Y. Zhao, X.-B. Zhang, Z.-X. Han, L. Qiao, C.-Y. Li, L.-X. Jian, G.-L. Shen, R.-Q. Yu, Anal. Chem. 2009, 81, 7022-7030.
34. N. Li, Y. Xiang, A. Tong, Chem. Commun. 2010, 46, 3363-3365
35. D. Wang, Y. Shiraishi, T. Hirai, Chem. Commun. 2011, 47, 2673-2675.
36. L.-F. Zhang, J.-L. Zhao, X. Zeng, L. Mu, X.-K. Jiang, M. Deng, J.-X. Zhang, G. Wei, Sens. Actuators B 2011, 160, 662-669
37. J. Fan, X. Liu, M. Hu, H. Zhu, F. Song, X. Peng, Anal. Chim. Acta 2012, 735, 107-113
38. M. Yu, M. Shi, Z. Chen, F. Li, X. Li, Y. Gao, J. Xu, H. Yang, Z. Zhou, T. Yi, C. Huang, Chem. Eur. J. 2008, 14, 6892-6900
39. C. Yu, J. Zhang, R. Wang, L. Chen, Org. Biomol. Chem. 2010, 8, 5277-5279.
40. M. R. Malachowski, M. Adams, N. Elia, A. L. Rheingold, R. S. Kelly, J. Chem. Soc. Dalton Trans. 1999, 0, 2177-2182
41. A. Benzekri, C. Cartier, J.-M. Latour, D. Limosin, P. Rey, M. Verdaguer, Inorg. Chim. Acta 1996, 252, 413-420
42. S. Kitagawa, M. Munakata, A. Higashie, Inorg. Chim. Acta 1984, 84, 79-84
43. M. M. Olmstead, W. K. Musker, R. M. Kessler, Inorg. Chem. 1981, 20, 151-157
44. C. F. Martens, A. P. H. J. Schenning, R. J. M. K. Gebbink, M. C. Feiters, J. G. M. van der Linden, J. Heck, R. J. M. Nolte, J. Chem. Soc. Chem. Commun. 1993, 0, 88-90
45. M. J. Schilstra, P. J. M. W. L. Birker, G. C. Verschoor, J. Reedijk, Inorg. Chem. 1982, 21, 2637-2644
46. P. J. M. W. L. Birker, J. Helder, G. Henkel, B. Krebs, J. Reedijk, Inorg. Chem. 1982, 21, 357-363.
47. M. Chaudhry, I. Persson, J. Chem. Soc. Faraday Trans. 1994, 90, 2243-2248
48. D. S. Gill, L. Rodehuser, J.-J. Delpuech, J. Chem. Soc. Faraday Trans. 1990, 86, 2847-2852
49. D. S. Gill, R. Srivastava, J. Chem. Soc. Faraday Trans. 1 1982, 78, 1533-1538
50. K. Kurnia, D. E. Giles, P. M. May, P. Singh, G. T. Hefter, Talanta 1996, 43, 2045-2051.